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氧化低密度脂蛋白和对氧磷酶 1 作为睡眠呼吸障碍患者冠心病的生物标志物。

Oxidized-LDL and paraoxonase-1 as biomarkers of coronary artery disease in patients with sleep-disordered breathing.

机构信息

Departamento de Biofísica, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

出版信息

Curr Med Chem. 2012;19(25):4359-66. doi: 10.2174/092986712802884312.

DOI:10.2174/092986712802884312
PMID:22934769
Abstract

UNLABELLED

Coronary Artery Disease (CAD) and

OBJECTIVES

Sleep Disordered Breathing (SDB) are both oxidative stress disorders. SDB intermittent hypoxia induces oxidative stress, and reduces NO(·) availability, causing endothelial dysfunction. Low-density lipoprotein (LDL) peroxidation is involved in atherosclerosis, and is reported in SDB. Oxidized LDL (ox-LDL) and malondialdehyde (MDA) are lipid peroxidation markers. High-density lipoprotein (HDL) presents antiatherosclerotic properties related to paraxonase-1 (PON-1) activity. PON-1 hydrolyseyses lipid peroxides as ox-LDL. This study compares the relationship of HDL and PON-1, the lipid peroxidation markers ox-LDL and MDA, and 8-OHdG DNA damage marker in the association of SDB and CAD.

DESIGN AND METHODS

29 controls and 27 cases with CAD (defined as > 30% coronary narrowing) patients were included. The apnea-hypopnea index (AHI), and several lipid and oxidative stress parameters were measured in these patients.

RESULTS

AHI is increased in CAD patients, and PON-1 activity and HDL levels are decreased. Regression analyseyses showed that lower PON-1 activity and higher ox-LDL levels are important CAD predictors, compared to HDL or MDA levels and present an age-dependent increase. Nitrites and nitrates, indirect NO(·) markers, are positive vs correlated with PON-1 and are negatively correlated to ox-LDL. SDB is not correlated to PON-1 activity decrease or ox-LDL increase. AHI is inversely correlated to HDL levels.

CONCLUSIONS

These results indicate that PON-1 and ox-LDL are important predictors of CAD, however they may not be directly related to SDB.

摘要

未标注

冠状动脉疾病(CAD)和

目的

睡眠呼吸紊乱(SDB)都是氧化应激紊乱。SDB 间歇性缺氧会引起氧化应激,降低一氧化氮(NO(·))的可用性,导致内皮功能障碍。低密度脂蛋白(LDL)的过氧化作用参与动脉粥样硬化,并在 SDB 中被报道。氧化型 LDL(ox-LDL)和丙二醛(MDA)是脂质过氧化的标志物。高密度脂蛋白(HDL)具有与对氧磷酶-1(PON-1)活性相关的抗动脉粥样硬化特性。PON-1 可水解脂质过氧化物如 ox-LDL。本研究比较了 SDB 和 CAD 之间的 HDL 和 PON-1、脂质过氧化标志物 ox-LDL 和 MDA 以及 8-OHdG DNA 损伤标志物的关系。

设计和方法

纳入 29 名对照者和 27 名 CAD 患者(定义为> 30%冠状动脉狭窄)。测量这些患者的呼吸暂停-低通气指数(AHI)和几个血脂和氧化应激参数。

结果

CAD 患者的 AHI 增加,PON-1 活性和 HDL 水平降低。回归分析表明,与 HDL 或 MDA 水平相比,较低的 PON-1 活性和较高的 ox-LDL 水平是 CAD 的重要预测因子,并且随年龄增长而增加。亚硝酸盐和硝酸盐是间接的 NO(·)标志物,与 PON-1 呈正相关,与 ox-LDL 呈负相关。SDB 与 PON-1 活性降低或 ox-LDL 增加无关。AHI 与 HDL 水平呈负相关。

结论

这些结果表明 PON-1 和 ox-LDL 是 CAD 的重要预测因子,但它们可能与 SDB 没有直接关系。

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